Evidence map›Paper›PMID 36149941›Full record

ArticleBlood advances2022

Production and nonclinical evaluation of an autologous iPSC-derived platelet product for the iPLAT1 clinical trial.

Naoshi Sugimoto, Sou Nakamura, Shin Shimizu, Akiko Shigemasa, Junya Kanda, Nobuki Matsuyama, Mitsunobu Tanaka, Tomoya Hayashi, Akihiro Fuchizaki, Masayuki Nogawa and 9 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
6.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Laboratory Assessment and Clinical Outlook forAnnals of laboratory medicine · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Induced pluripotent stem cell-derived platelets kill multidrug-resistantResearch and practice in thrombosis and haemostasis · 2026
    Article
  9. Glycan Markers of Pluripotent Stem Cells.Advances in experimental medicine and biology · 2026
    Review
  10. Review
  11. Platelet Transfusion for Patients with Cancer: An Update.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2025
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Frontiers in immunology · 2025
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 1 country.

Naoshi SugimotoDepartment of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.ORCID 0000-0002-7271-9175
Sou NakamuraDepartment of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.ORCID 0000-0002-5601-9777
Shin ShimizuDepartment of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
Akiko ShigemasaDepartment of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
Junya KandaDepartment of Hematology, Kyoto University Hospital, Kyoto, Japan.ORCID 0000-0002-6704-3633
Nobuki MatsuyamaJapanese Red Cross Kinki Block Blood Center, Osaka, Japan.
Mitsunobu TanakaJapanese Red Cross Kinki Block Blood Center, Osaka, Japan.ORCID 0000-0002-9024-6818
Tomoya HayashiJapanese Red Cross Kinki Block Blood Center, Osaka, Japan.ORCID 0000-0002-1776-0052
Akihiro FuchizakiJapanese Red Cross Kinki Block Blood Center, Osaka, Japan.ORCID 0000-0003-3387-1817
Masayuki NogawaCentral Blood Institute, Blood Service Headquarters, Japanese Red Cross Society, Tokyo, Japan.ORCID 0000-0002-4835-2545
Naohide WatanabeDivision of Hematology, Keio University School of Medicine, Tokyo, Japan.
Shinichiro OkamotoDivision of Hematology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-6257-4152
Makoto HandaCenter for Transfusion Medicine & Cell Therapy, Keio University School of Medicine, Tokyo, Japan.
Akira SawaguchiDepartment of Anatomy, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
Dai MomoseDepartment of Hematology, Osaka General Hospital of West Japan Railway Company, Osaka, Japan.
Ki-Ryang KohDepartment of Hematology, Osaka General Hospital of West Japan Railway Company, Osaka, Japan.
Yoshihiko TaniJapanese Red Cross Kinki Block Blood Center, Osaka, Japan.
Akifumi Takaori-KondoDepartment of Hematology, Kyoto University Hospital, Kyoto, Japan.ORCID 0000-0001-7678-4284
Koji EtoDepartment of Clinical Application, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.ORCID 0000-0002-5863-7122
Japanese Red Cross Society, Japan · JPKyoto University · JPKeio University · JPKyoto University Hospital · JPUniversity of Miyazaki · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Donor-derived platelets are used to treat or prevent hemorrhage in patients with thrombocytopenia. However, ∼5% or more of these patients are complicated with alloimmune platelet transfusion refractoriness (allo-PTR) due to alloantibodies against HLA-I or human platelet antigens (HPA). In these cases, platelets from compatible donors are necessary, but it is difficult to find such donors for patients with rare HLA-I or HPA. To produce platelet products for patients with aplastic anemia with allo-PTR due to rare HPA-1 mismatch in Japan, we developed an ex vivo good manufacturing process (GMP)-based production system for an induced pluripotent stem cell-derived platelet product (iPSC-PLTs). Immortalized megakaryocyte progenitor cell lines (imMKCLs) were established from patient iPSCs, and a competent imMKCL clone was selected for the master cell bank (MCB) and confirmed for safety, including negativity of pathogens. From this MCB, iPSC-PLTs were produced using turbulent flow bioreactors and new drugs. In extensive nonclinical studies, iPSC-PLTs were confirmed for quality, safety, and efficacy, including hemostasis in a rabbit model. This report presents a complete system for the GMP-based production of iPSC-PLTs and the required nonclinical studies and thus supports the iPLAT1 study, the first-in-human clinical trial of iPSC-PLTs in a patient with allo-PTR and no compatible donor using the autologous product. It also serves as a comprehensive reference for the development of widely applicable allogeneic iPSC-PLTs and other cell products that use iPSC-derived progenitor cells as MCB.

Indexed as

Antigens, Human PlateletHematopoietic Stem Cell TransplantationInduced Pluripotent Stem CellsThrombocytopeniaAnimalsBlood PlateletsHumansPlatelet TransfusionRabbitsAntigens, Human Platelet

Identifiers

PMID36149941
PMCPMC9706535
OpenAlexW4296844945

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.